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Chick-Fil-A
Updated: January 21, 2021 12:00 PM
Covid-19 OSHA Complaint, Chick-Fil-A, Inc., 4944 Kingston Pike, KNOXVILLE, TN, 37919, USA
Chick-Fil-A, Inc., 4944 Kingston Pike, KNOXVILLE, TN, 37919, USA
January 21, 2021 12:00 PM
“1) Employees have been exposed to other employees who tested positive for COVID-19 and the employer has not informed the exposed employees.
Alleged Hazards: 1, Employees Exposed: 80
Source: Osha.gov | Receipt Date: 2020-12-28 See Less”
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2 individuals tested positive for Covid-19, Chick-fil-A, 5260 S Wadsworth Blvd, Littleton, CO 80123
Chick-fil-A, 5260 S Wadsworth Blvd, Littleton, CO 80123
December 23, 2020 12:00 PM
“2 individuals at Chick-fil-a- Belleview Shores in Jefferson county tested positive for Covid-19. The outbreak began on 11/12/2020
Source: colorado.gov See Less”
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3 employees tested positive for Covid-19, CHICK-FIL-A, 5009 MONTGOMERY BLVD NE, ALBUQUERQUE
CHICK-FIL-A, 5009 MONTGOMERY BLVD NE, ALBUQUERQUE
December 22, 2020 12:00 PM
“Multiple employees(3) at CHICK-FIL-A in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 12/23/2020,
Source: env.nm.gov See Less”
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2 employees tested positive for Covid-19, CHICK-FIL-A, 1600 GIBSON BLVD SE, ALBUQUERQUE
CHICK-FIL-A, 1600 GIBSON BLVD SE, ALBUQUERQUE
December 16, 2020 12:00 PM
“Multiple employees(2) at CHICK-FIL-A in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 12/17/2020,
Source: env.nm.gov See Less”
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2 additional individuals tested positive for Covid-19, Chick-fil-A, 5260 S Wadsworth Blvd, Littleton, CO 80123
Chick-fil-A, 5260 S Wadsworth Blvd, Littleton, CO 80123
December 10, 2020 12:00 PM
“2 additional individuals at Chick-fil-a- Belleview Shores in Jefferson county tested positive for Covid-19. The outbreak began on 11/12/20
Source: colorado.gov See Less”
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2 employees tested positive for Covid-19, CHICK-FIL-A, 1600 GIBSON BLVD SE, ALBUQUERQUE
CHICK-FIL-A, 1600 GIBSON BLVD SE, ALBUQUERQUE
December 10, 2020 12:00 PM
“Multiple employees(2) at CHICK-FIL-A in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 12/09/2020,
Source: env.nm.gov See Less”
Helpful
1 Additional individual tested positive for Covid-19, Chick-fil-A, 5260 S Wadsworth Blvd, Littleton, CO 80123
Chick-fil-A, 5260 S Wadsworth Blvd, Littleton, CO 80123
December 7, 2020 12:00 PM
“1 Additional individual at Chick-fil-a- Belleview Shores in Jefferson county tested positive for Covid-19. The outbreak began on 11/12/20
Source: colorado.gov See Less”
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Covid-19 OSHA Complaint, Chick-fil-A, 3675 S US Hwy 41, TERRE HAUTE, IN, 47802, USA
Chick-fil-A, 3675 S US Hwy 41, TERRE HAUTE, IN, 47802, USA
December 2, 2020 12:00 PM
“Heat stress and covid risk. Employees are outside on a daily basis less than six feet away from guests and co workers. Most guests don't even bother to wear mask or face coverings.
Source: Osha.gov | Receipt Date: 2020-06-30 See Less”
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4 employees tested positive for Covid-19, Chick-fil-A, 2400 Cerrillos Rd, Santa Fe, NM, USA
Chick-fil-A, 2400 Cerrillos Rd, Santa Fe, NM, USA
December 1, 2020 12:00 PM
“Multiple employees(4) at CHICK-FIL-A in SANTA FE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 12/02/2020,
Source: env.nm.gov See Less”
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3 individuals tested positive for Covid-19, Chick-fil-A, 2580 Coalton Rd, Superior, CO 80027, USA
Chick-fil-A, 2580 Coalton Rd, Superior, CO 80027, USA
November 27, 2020 12:00 PM
“3 individuals at Chick-Fil-A- Flatiron in Broomfield county tested positive for Covid-19. The outbreak began on 10/27/20
Source: colorado.gov See Less”
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Moderna COVID-19 vaccine, Sevierville, TN, USA
Symptoms: Headache
Chills
Fatigue
Joint Pain
Muscle Pain
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Sevierville, TN, USA
January 22, 2021 1:14 PM
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West Virginia, USA
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Helpful
2 people found this review helpful
January 17, 2021 11:59 PM
“The FSA announced the recall of several dog food products by Mars Petcare UK because they may contain high levels of vitamin D which exceed the maximum permitted intake.
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High levels of vitamin D fed to a pet over a short period (weeks/months) should not cause undue concern. Over a longer period of feeding, ingestion of elevated levels can lead to potential dog health issues. Vitamin D, when consumed at very high levels, can lead to serious health issues in dogs including renal dysfunction.
Check the full recall details on the FSA website food.gov.uk
Source: FSA See Less”
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Moderna Covid19 vaccine, New Jersey, USA
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December 30, 2020 10:00 PM
“Company name: Sportmix
Brand name: Sportmix
Product recalled: Dog and Cat Food
Reason of the recall: Elevated levels of aflatoxin
FDA Recall date: December 30, 2020
Recall details: Midwestern Pet Foods, Inc., of Evansville, IN is issuing a voluntary recall of the below-listed dog and cat food p... See Moreroducts due to tests indicating levels of Aflatoxin that exceed acceptable limits. Products were distributed nationally to online distributors and retail stores. Aflatoxin is a toxin produced by the mold Aspergillus flavus, which can grow on corn and other grains used as ingredients in pet food. At high levels, aflatoxin can cause illness and death in pets.
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Retailers and distributors should immediately pull recalled lots from their inventory and shelves. Do not sell or donate the recalled products. Retailers are encouraged to contact consumers who have purchased the recalled products if you have the means to do so (frequent buyer cards, etc.).
Pet parents: do not feed the recalled products to your pets or any other animals. Destroy the products in a way that children, pets, and wildlife cannot access them. Wash and sanitize pet food bowls, cups, and storage containers. Contact Midwestern Pet Foods Consumer Affairs at 800-474-4163, ext. 455 from 7AM to 4PM Central Time, Monday through Friday, or by email at info@midwesternpetfoods.com for additional information. This is a voluntary recall conducted in cooperation with the U.S. Food and Drug Administration.
Recalled lot codes are as follows:
- 50# Sportmix Energy Plus Lots Exp 03/02/22/05/L2, 03/02/22/05/L3, 03/03/22/05/L2
- 44# Sportmix Energy Plus Lots 03/02/22/05/L3
- 50# Sportmix Premium High Energy Lots 03/03/22/05/L3
- 44# Sportmix Premium High Energy Lots 03/03/22/05/L3
- 31# Sportmix Original Cat Lots 03/03/22/05/L3
- 15# Sportmix Original Cat Lots 03/03/22/05/L2, 03/03/22/05/L3
Products may be identified as follows (see pictures below).
Check the full recall details on fda.gov
Source: FDA See Less”
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January 8, 2021 6:01 PM
“Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi
Product recalled: Ketorolac Tromethamine Injection, USP, 30 mg/mL
Reason of the recall: Presence of particulate matter
FDA Recall date: January 08, 2021
Recall details: Fresenius Kabi USA is voluntarily recalling a single lot of Ketoro... See Morelac Tromethamine Injection, USP, 30 mg/mL, 1 mL fill in a 2 mL amber vial to the user level due to the presence of particulate matter. Particulate matter was found in reserve sample vials. No adverse event reports have been received for the recalled lot, which was produced and sold in 2019.
Administration of products containing particulate matter could obstruct blood vessels and result in local irritation of blood vessels, swelling at the site of injection, a mass of tissue that could become inflamed and infected, blood clots traveling to the lung, scarring of the lung tissues, and allergic reactions that could lead to life-threatening consequences.
Ketorolac Tromethamine, a nonsteroidal anti-inflammatory drug, is indicated for the short-term (up to 5 days in adults) management of moderately severe acute pain that requires analgesia at the opioid level. The total combined duration of use of oral Ketorolac Tromethamine and Ketorolac Tromethamine Injection should not exceed 5 days. Listed below is a table of the recalled lot distributed nationwide in the United States to wholesalers, distributors, hospitals, and pharmacies between March 28, 2019 and September 3, 2019.
Product Name/Product size: Ketorolac Tromethamine Injection, USP, 30mg / mL, 1 mL fill in a 2 mL amber vial
NDC Number: 63323-162-01
Product Code: 160201
Batch Number: 6121083
Expiration Date: 02/2021
First Ship Date: 03/28/2019
Last Ship Date: 09/03/2019
Fresenius Kabi is notifying its distributors and customers by letter and asking customers and distributors to check their stock immediately and to quarantine and discontinue the use and distribution of any affected product. Distributors should notify their customers and direct them to quarantine and discontinue distributing or dispensing the affected lot, and to return the product to Fresenius Kabi.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA See Less”
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2 people found this review helpful